Research Support

About the role

The Clinical Addictions Research Laboratory (CARL) was incepted in 1997 under the direction of Andrea King, PhD., Professor in the Department of Psychiatry and Behavioral Neuroscience at the University of Chicago. The overarching mission of CARL is two-folded: 1) To determine factors that lead to excessive use of alcohol, tobacco, and other substances, 2) To develop more effective interventions in the treatment of substance use disorders.

Responsibilities

• Responsible for all aspects of research projects, including study recruitment and retention, participant screening and enrollment, data entry and database management, and study-related communications among key personnel and participants.
• Facilitate and monitor data collection - including obtaining subjective, objective (e.g. vital sign readings, etc.), biological (e.g. urine, blood, saliva, etc.), and performance (e.g. fine motor tasks, neurocognitive tasks, eye movement tasks, etc.) measures.
• Provide administrative support (i.e. petty cash distribution, equipment inventory and maintenance, scientific literature reviews, etc.) and maintain detailed records of study and lab standard operating procedures.
• Aid in data analysis and development of tables, graphs, and charts in preparation for reports, manuscripts, and presentations.
• Follow all relevant current local, state, & federal laws, regulations, guidance, policy & procedure developed by the University of Chicago Institutional Review Board (IRB), Food & Drug Administration (FDA) Code of Federal Regulations (CFR), & the International Conference on Harmonization (ICH).
• Conduct screenings and participant interviews as needed; ensure database management, entry and verification of measures not obtained by computer; and supervise and schedule sessions.
• Perform clinical interviews as needed, assist the lab manager on regulatory paperwork, and schedule and manage all disbursements and receipts.
• Manage study supply inventory and ordering.
• Create subject mailings for materials related to their participation in the trial, including study medications and saliva drug screens.
• Comply with institution, state and federal regulatory policies, procedures, directives, and mandates.
• Perform routine or standardized laboratory duties by collecting data in support of research projects under direct supervision.
• Collect and enter data. Assist in analysis of data and with preparation of reports, manuscripts and other documents.
• Perform other related work as needed.

Education

• Minimum requirements include vocational training, apprenticeships or the equivalent experience in related field (not typically required to have a four-year degree).
• Minimum requirements include knowledge and skills developed through < 2 years of work experience in a related job discipline.

Technical Skills

• Proficiency in MS Excel and electronic data capture (Redcap).
• Experience in coding and statistical programs (R, Python, Java, SPSS, STATA, etc.).
• Experience in interviewing and conducting experimental sessions in behavioral research.

Preferred Qualifications

• Experience working in a complex academic medical center.